Reacción #80334

Ecuación de reacción

sodium hydride

N-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-3-mercaptopropionamide

ethylene chlorohydrin

→

title compound

Rendimiento 65.0%

N-[4-(4-Piperidinomethyl-2 -pyridyloxy)-cis-2 -butenyl]-3-(2-hydroxyethylthio)propionamide

Rendimiento 65.0%

Disolventes

dimethylformamide

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturacooling
2. 2
   workup.STIRRINGThe reaction mixture was stirred at room temperature for 15 minutes
3. 3
   Extracciónextracted with ethyl acetate
4. 4
   ConcentraciónThe extract was concentrated by evaporation under reduced pressure
5. 5
   Otrothe residue thus obtained
6. 6
   Otrowas purified by column chromatography through silica gel
7. 7
   workup.ADDITIONby volume mixture of methanol and methylene chloride as the eluent

Procedimiento

105 mg of sodium hydride (as a 55% w/w dispersion in mineral oil) were added, whilst ice-cooling and in an atmosphere of nitrogen, to a solution of 0.76 g of N-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-3-mercaptopropionamide (prepared as described in Preparation 3) in 24 ml of dimethylformamide, and the resulting mixture was stirred at room temperature for 30 minutes. At the end of this time, 0.16 ml of ethylene chlorohydrin were added to the reaction mixture, whilst ice-cooling. The reaction mixture was stirred at room temperature for 15 minutes, after which it was poured into ice-water and extracted with ethyl acetate. The extract was concentrated by evaporation under reduced pressure, and the residue thus obtained was purified by column chromatography through silica gel, using a 1:9 by volume mixture of methanol and methylene chloride as the eluent, to give 0.56 g of the title compound as an oil in a 65% yield.

Fuente